Ruifrok P G
Naunyn Schmiedebergs Arch Pharmacol. 1982 Jun;319(3):185-8. doi: 10.1007/BF00495863.
In a previous article [Naunyn-Schmiedeberg's Arch Pharmacol (1981) 316:266-272] transport of a number of organic ions across lipid bilayers was investigated using single bilayer liposomes. In this investigation the translocation of structurally closely related barbiturates across lipid bilayers is studied. The anionic form of the barbiturates can pass lipid bilayers, provided that the lipophilicity of the 5,5-disubstituted side chain is high enough. This permeability of barbiturates in the ionized form explains their uncoupling action of the oxidative phosphorylation and the deviations from the pH-partition theory found in absorption processes.
在之前的一篇文章中[《瑙尼恩-施米德贝格药理学文献》(1981年)第316卷:266 - 272页],使用单层脂质体研究了多种有机离子跨脂质双层的转运。在本研究中,对结构密切相关的巴比妥类药物跨脂质双层的转运进行了研究。巴比妥类药物的阴离子形式能够穿过脂质双层,前提是5,5 - 二取代侧链的亲脂性足够高。巴比妥类药物以离子化形式的这种通透性解释了它们对氧化磷酸化的解偶联作用以及在吸收过程中发现的与pH分配理论的偏差。